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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 489744생성일: 2026년 10월 25일

4-Toluenesulfonyl chloride → (2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonate

https://huagongshe.com/reaction/489744

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물Sodium BicarbonateHCID 516892—
반응물(2S)-(4E)-5-(3-Pyridyl)-4-penten-2-olHCID 20655737—
용매TriethylamineHCID 8471—
생성물(2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonateHCID 8746599468.6%

반응 단계

Under a nitrogen atmosphere, p-toluenesulfonyl chloride (7.01 g, 36.77 mmol) was added to a stirring solution of (2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol (3.00 g, 18.38 mmol) in dry triethylamine (20 mL) at 0° C. After stirring and warming to ambient temperature over 18 h, the mixture was stirred with cold, saturated NaHCO3 solution (50 mL) for 1 hour and extracted with chloroform (3×50 mL). The combined chloroform extracts were dried (K2CO3), filtered, and concentrated by rotary evaporation to afford a thick, dark-brown mass (˜7 g). The crude product was purified by column chromatography on silica gel, eluting with chloroform-acetone (98:2, v/v) to afford 4.00 g (68.6%) of a light-brown syrup.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06979695B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-078c4ce6f95e4e448f83fe237a725ad8
출처 메모uspto-grants-2005_12